APA

Dotti M. T., Buccoliero R., Lee A., Gorospe J. R., Flint D., Galluzzi P., Bianchi S., D'Eramo C., Naidu S., Federico A. & Brenner M. (20090820). An infantile case of Alexander disease unusual for its MRI features and a GFAP allele carrying both the p.Arg79His mutation and the p.Glu223Gln coding variant. : Journal of neurology.

Chicago

Dotti Maria Teresa, Buccoliero Rosaria, Lee Andrew, Gorospe J Raphael, Flint Daniel, Galluzzi Paolo, Bianchi Silvia, D'Eramo Camilla, Naidu Sakkubai, Federico Antonio and Brenner Michael. 20090820. An infantile case of Alexander disease unusual for its MRI features and a GFAP allele carrying both the p.Arg79His mutation and the p.Glu223Gln coding variant. : Journal of neurology.

Harvard

Dotti M. T., Buccoliero R., Lee A., Gorospe J. R., Flint D., Galluzzi P., Bianchi S., D'Eramo C., Naidu S., Federico A. and Brenner M. (20090820). An infantile case of Alexander disease unusual for its MRI features and a GFAP allele carrying both the p.Arg79His mutation and the p.Glu223Gln coding variant. : Journal of neurology.

MLA

Dotti Maria Teresa, Buccoliero Rosaria, Lee Andrew, Gorospe J Raphael, Flint Daniel, Galluzzi Paolo, Bianchi Silvia, D'Eramo Camilla, Naidu Sakkubai, Federico Antonio and Brenner Michael. An infantile case of Alexander disease unusual for its MRI features and a GFAP allele carrying both the p.Arg79His mutation and the p.Glu223Gln coding variant. : Journal of neurology. 20090820.